Custom Pharmaceuticals Ltd are developing a new Hormonal OSD Manufacturing Facility in Hove, UK. The client required Validation support during Phase 1 of the project.
The GMP Group produced the Validation Master Plan for Custom Pharma, and we are currently on-site, executing the master plan and giving continued validation support to the client. This has included the preparation of commissioning and qualification plans, the preparation of validation report templates, and on-site commissioning for all M&E services, BMS and FMS installations, amongst other tasks.
We continue to have a positive working relationship with Custom Pharma in the Validation of this project, and will be assisting with the requalification of all existing equipment.
